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Summary ExpressionExpr. PhenotypesPheno. Gene Literature (0)Lit. (0) GO Terms (13)GO (13) Nucleotides (96)Nucl. (96) Proteins (44)Prot. (44) Interactants (88)Interact. (88) Wiki
XB-GENEPAGE-941636
???displayGene.symbol???:
 opa3

???displayGene.name???: 
optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)

???displayGene.synonyms???
( Nomenclature history )

???displayGene.geneFunction???
Predicted coiled-coil protein

AI Protein Function :
opa3 encodes a mitochondrial inner membrane protein that participates in melanosome biogenesis and pigment cell development; it localizes to mitochondria and is required for proper formation of melanop...[+]


InterPro :
OPA3-like

???displayGene.geneInteractants???
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Diseases: 


Disease Ontology:
3-methylglutaconic aciduria type 3 [+]

MIM:
3-METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3 [+]

External Links:
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???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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